Etiology and clinical features of children with bronchiectasis in China: A 10-year multicenter retrospective study

Hao Wang1,2, Bao-Ping Xu1,2, Yan-Min Bao3

  • 1Beijing Children's Hospital, Capital Medical University, Beijing, China.

Insights

This study identified post-infective causes, primary immunodeficiency, and primary ciliary dyskinesia (PCD) as common etiologies for bronchiectasis in Chinese children. Clinical features can help indicate specific underlying causes.

Area of Science:

  • Pediatric Pulmonology
  • Respiratory Medicine
  • Medical Etiology Research

Background:

  • Bronchiectasis in children presents a significant clinical challenge.
  • Understanding the spectrum of causes and clinical features is crucial for effective management.

Purpose of the Study:

  • To investigate the etiological spectrum of bronchiectasis in Chinese children.
  • To characterize the clinical presentation and high-resolution computed tomography (HRCT) findings.

Main Methods:

  • A multicenter retrospective study involving 193 pediatric cases across 13 centers in China (2008-2017).
  • Inclusion required confirmed clinical and HRCT diagnostic criteria by two radiologists.
  • Data analysis was performed on enrolled cases meeting specific criteria.

Main Results:

  • An underlying etiology was identified in 87% of cases, with post-infective causes (46%), primary immunodeficiency (14%), and primary ciliary dyskinesia (PCD) (13%) being most frequent.
  • Common symptoms included cough, sputum production, and fever during exacerbations; 19% had limited exercise tolerance and 30% showed growth limitations.
  • HRCT revealed diffuse bronchiectasis in 126 cases, predominantly affecting lower and right middle lobes; positive cultures were found in approximately 30%.

Conclusions:

  • A majority of pediatric bronchiectasis cases in China have identifiable underlying etiologies.
  • Post-infective causes, primary immunodeficiency, and PCD are the leading contributors.
  • Specific clinical manifestations may suggest particular etiological origins.
Abstract

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